Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Eflornithine
Drug ID BADD_D00751
Description Eflornithine is a prescription drug indicated in the treatment of facial hirsutism (excessive hair growth). Eflornithine hydrochloride cream for topical application is intended for use in women suffering from facial hirsutism and is sold by Allergan, Inc. under the brand name Vaniqa. Eflornithine for injection against sleeping sickness was manufactured by Sanofi Aventis and sold under the brand name Ornidyl in the USA. It is now discontinued. Eflornithine is on the World Health Organization's List of Essential Medicines.
Indications and Usage Eflornithine is indicated in the treatment of facial hirsutism (excessive hair growth).
Marketing Status Prescription; Discontinued
ATC Code D11AX16; P01CX03
DrugBank ID DB06243
KEGG ID D07883
MeSH ID D000518
PubChem ID 3009
TTD Drug ID D0X7JR
NDC Product Code Not Available
Synonyms Eflornithine | DL-alpha-Difluoromethylornithine | DL alpha Difluoromethylornithine | alpha-Difluoromethylornithine | alpha Difluoromethylornithine | alpha-Difluoromethyl Ornithine | Ornithine, alpha-Difluoromethyl | alpha Difluoromethyl Ornithine | Difluoromethylornithine | MDL-71,782 A | MDL 71,782 A | MDL71,782 A | Ornidyl | Vaniqa | Eflornithine Monohydrochloride, Monohydrate | Eflornithine Hydrochloride | RMI 71782
Chemical Information
Molecular Formula C6H12F2N2O2
CAS Registry Number 70052-12-9
SMILES C(CC(C(F)F)(C(=O)O)N)CN
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Pruritus23.03.12.001--
Pseudofolliculitis barbae23.02.06.009--Not Available
Rash23.03.13.001--Not Available
Rash maculo-papular23.03.13.004--
Rash papular23.03.13.017--Not Available
Rash pustular23.03.10.003; 11.01.12.002--
Rosacea23.02.08.001--Not Available
Seborrhoeic dermatitis23.03.04.018--Not Available
Sensory loss17.02.07.007--Not Available
Skin disorder23.03.03.007--Not Available
Skin irritation23.03.04.009--Not Available
Tenderness08.01.08.005--Not Available
Vertigo04.04.01.003; 17.02.12.002--
Skin tightness23.03.03.018--Not Available
Ingrown hair23.02.06.008--Not Available
Skin burning sensation23.03.03.021; 17.02.06.009--Not Available
Hypoaesthesia oral17.02.06.021; 07.05.05.003--Not Available
Decreased appetite08.01.09.028; 14.03.01.005--
Skin haemorrhage24.07.06.009; 23.06.07.001--Not Available
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